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N-STRAINED SIGNED

Nitrogen-Radical-Based Radical Strain-Release Strategies for the Divergent Assembly of Polyfunctionalized 3D-Building Blocks

Total Cost €

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EC-Contrib. €

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Partnership

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 N-STRAINED project word cloud

Explore the words cloud of the N-STRAINED project. It provides you a very rough idea of what is the project "N-STRAINED" about.

generating    pentylamines    substantially    react    difficulties    introduce    direct       structural    polyfunctionalized    transferring    agrochemicals    flat    2d    nitrogenated    basis    aromatics    quest    career    envisioned    propellane    photoredox    strain    life    group    disclosed    central    platform    manchester    almost    reaction    saturated    urgent    compounds    small    endeavour    bonds    pentyl    preparing    medicinal    strained    preparation    evolve    containing    clinical    eg    radicals    pharmaceutical    capitalizes    release    prepared    materials    potency    nitrogen    limited    strategic    facilitated    expand    architectures    lives    university    strategies    plan    designing    assemble    modifying    explore    manipulate    replace    innovative    construction    valuable    blocks    chemical    training    implications    drugs    scientific    building    reactivity    chemistry    space    invention    form    discover    generate    disseminating    divergent    molecules    host    severely    bicyclo    shaped    photocatalysis    3d    explores    synthetic    organic    sharing    continuous    bioisoter    introducing    motif    underpin    hydrocarbons    ways   

Project "N-STRAINED" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF MANCHESTER 

Organization address
address: OXFORD ROAD
city: MANCHESTER
postcode: M13 9PL
website: www.manchester.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2021-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF MANCHESTER UK (MANCHESTER) coordinator 212˙933.00

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 Project objective

Nitrogen-containing compounds underpin every aspect of our life: they form the structural basis of almost all drugs, agrochemicals and materials. The invention of methods to form C–N bonds is of strategic importance to discover and evolve molecules with direct implications on our lives. Central to this quest is designing synthetic strategies able to explore novel areas of chemical space. As the pharmaceutical sector is now aware of the greater clinical success of molecules with 3D architectures, developing methods able to assemble 3D-shaped and saturated building blocks is a topic of continuous scientific endeavour. The small and strained bicyclo[1.1.1]pentyl motif has been identified as a valuable bioisoter to replace flat (2D) aromatics and improve the potency of lead molecules. However, difficulties in preparing and modifying this structural element have severely limited its use in medicinal chemistry. There is an urgent need to develop novel methods that can effectively manipulate and introduce this motif into organic compounds. This project seeks to substantially expand the fields of photocatalysis and nitrogen-radicals by introducing the concept of “photoredox strain-release”: a novel reactivity that explores the ability of nitrogen-radicals to react with strained hydrocarbons (eg propellane) and enable a unique preparation of polyfunctionalized bicyclo[1.1.1]pentylamines. This research capitalizes on recent developments of the host group that has disclosed 2 novel ways to effectively generate nitrogen radicals. This reactivity will be integrated with other reaction platform allowing the divergent 1-step construction of many important nitrogenated 3D-building blocks that cannot be prepared by any other method. The development of such an innovative and ambitious project at the University of Manchester will be facilitated by generating, transferring, sharing and disseminating knowledge, and will enhance my future career following the training plan envisioned.

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